Method of securing a patient onto an operating table when the patient is in a position such as the trendelenburg position and apparatus therefor including a kit

ABSTRACT

A method of securing a patient onto an operating table when the patient is in a position such as the trendelenburg position and apparatus therefor including a kit. A viscoelastic pad is used to support and hold a patient on a medical procedure table during a medical procedure performed while the table, and thus the patient lying thereon, is in an inclined position, such as the Trendelenburg position. The viscoelastic pad has characteristics which promote a minimization of pressure forces on the patient&#39;s body, as well as promote a secure cushioning and holding of the patient in a desired position on the table, in order to minimize injury to the patient.

CONTINUING APPLICATION DATA

The present application is a continuation of U.S. patent applicationSer. No. 14/881,274, filed Oct. 13, 2015, which is a continuation ofU.S. patent application Ser. No. 13/957,778, filed on Aug. 2, 2013,which issued as U.S. Pat. No. 9,161,876 on Oct. 20, 2015, which is acontinuation of U.S. patent application Ser. No. 13/773,290, filed onFeb. 21, 2013, which issued as U.S. Pat. No. 8,511,314 on Aug. 20, 2013,which is a continuation of U.S. patent application Ser. No. 13/737,552,filed on Jan. 9, 2013, which issued as U.S. Pat. No. 8,464,720, whichissued on Jun. 18, 2013, which is a continuation-in-part of U.S. patentapplication Ser. No. 13/346,852, filed on Jan. 10, 2012. U.S. patentapplication Ser. No. 13/773,290 also claims the benefit of U.S.Provisional Patent Application No. 61/654,339, filed on Jun. 1, 2012.

BRIEF DESCRIPTION OF THE DRAWINGS

The present application is explained in greater detail below withreference to the accompanying drawings:

FIG. 1 shows a top view of a Trendelenburg pad of the presentapplication comprising fasteners;

FIG. 2 shows a bottom view of the Trendelenburg pad as seen in FIG. 1;

FIGS. 3A and 3B show fasteners configured to hold the Trendelenburg padon the operating table;

FIG. 4 shows a Trendelenburg pad of the present disclosure secured to anoperating table and having a patient positioned thereon and also shows amethod of use;

FIG. 5 shows a Trendelenburg pad of the present disclosure having theimpression of a patient therein;

FIG. 6 shows a Trendelenburg pad of the present disclosure secured to anoperating table in the Trendelenburg position and having a patientpositioned thereon;

FIG. 7 shows a figure disposed on a Trendelenburg pad of the presentapplication;

FIG. 8 is a block diagram of a robotic surgery system to performminimally invasive robotic surgical procedures using one or more roboticsurgical arms with a strap drive train;

FIG. 9 a perspective view of the robotic patient-side system of FIG. 8with the one or more robotic surgical arms having the strap drive train;

FIG. 10 shows an example of robotic surgery; and

FIG. 11 is a representation of a table inclined at a forty-five degreeangle.

DESCRIPTION OF EMBODIMENT OR EMBODIMENTS

During performance of some medical procedures, such as surgicaloperations, a patient may be placed on a support or operating tablewhich is oriented horizontally, that is, perpendicularly with respect tothe vertical. However, depending on the medical procedure, it may bemore advantageous to orient the support or operating table, and thus thepatient, at an incline with respect to the horizontal. For medicalprocedures relating to the lower body, such as, for example, abdominalor gynecological operations, the Trendelenburg position may be used.This position involves a patient first lying horizontally on a supporttable. The operating table or a portion thereof is then inclined suchthat the head and upper torso of the patient is at a vertically lowerposition than the pelvic region and/or legs of the patient, as shown,for example, in FIG. 6. In general, the support table is inclined suchthat the patient's head and upper torso is lowered from the horizontalanywhere in a range of approximately five, ten, or fifteen degrees toapproximately twenty, thirty, or forty-five degrees or more, in a steepTrendelenburg position, in one degree increments or fractions of onedegree increments. In addition to the positive Trendelenburg position,there is a negative or reverse Trendelenburg position, where the headand upper torso is at a vertically higher position than the pelvicregion and/or legs of the patient. As used herein, the phraseTrendelenburg position should be understood as referring to bothpositions.

The present application discloses the use of a viscoelastic foam pad,such as shown in FIG. 1, to assist in holding the patient in a desiredposition on an inclined support table, such as in the Trendelenburgposition, and to assist in minimizing sliding, shifting, or similarundesirable movements of the patient on the support table, whichmovements could be disruptive to a medical procedure being performed onthe patient. The viscoelastic foam also cushions and supports thepatient while promoting a distribution of pressure forces across thepatient's body to reduce and/or minimize damage to nerves and/or tissuefrom concentrated pressure forces. For example, the viscoelastic foamwill minimize or can eliminate brachial plexopathy, including pain,decreased movement, or decreased sensation in the arm and shoulder byminimizing pressure to a patient's neck, arms, and/or shoulders, andthereby minimizing or reducing a nerve event. In at least one possibleembodiment, the viscoelastic foam has characteristics which are selectedto promote the preceding desired effects, which will be discussed in thefollowing paragraph. All of the characteristics discussed in thefollowing paragraph are according to at least one possible embodiment,and it should be understood that any one or more of the characteristicscould be combined with any one or more of the characteristics accordingto at least one possible embodiment, and any ranges disclosed in thefollowing paragraph are to be understood as including any value therein,including increments of tenths and hundredths of the particular range.

The rate of recovery, that is, the time required for a viscoelastic foamto return to its starting shape, is in the range of approximately 2-10seconds for approximately 50 percent to 80 percent recovery afterdeformation caused by placing an adult torso on an approximately oneinch thick layer of viscoelastic foam. The rate of recovery is in therange of approximately 6-15 seconds for approximately 80 percent to 90percent recovery after deformation caused by placing an adult torso onan approximately one inch thick layer of viscoelastic foam. The rate ofrecovery is in the range of approximately 10-35 seconds for 100 percentrecovery after deformation caused by placing an adult torso on anapproximately one inch thick layer of viscoelastic foam. The ballrebound of the viscoelastic foam is in the range of less than orsubstantially less than approximately one percent to approximately onepercent or several percent, or is in the range of or approximately inthe range of 0.1 percent to 1.9 percent, or up to 3 percent or 5percent, and as much as several percent. The compression set (theresidual compression of the foam after twenty-two hours at seventydegrees Celsius) of the viscoelastic foam, for a 25 percent compressionof the foam, is in the range of less than one percent or tenths of apercent, such as, for example, less than 0.4 percent or 0.3 percent, toseveral percent. The compression set of the viscoelastic foam, for afifty percent compression of the foam, is in the range of less than onepercent or tenths of a percent, such as, for example, less than 0.5percent, to several percent. The indentation force deflection of theviscoelastic foam, at a 25 percent deflection, is in the range ofseveral pounds of force to tens of pounds of force, such as in the rangeof approximately 10 to approximately 15 pounds, or in the range ofapproximately 7 to approximately 18 pounds, or is in the range ofapproximately 12 pounds, such as, for example, 11.7, 11.8, 11.9, 12.0,12.1, 12.2, 12.3, and 12.4 pounds. The coefficient of static frictionbetween the viscoelastic foam and the surface of a support table isgreater than 0.2, or is in the range of approximately 0.2 or 0.5 toapproximately 0.7 or 1.0. The viscoelastic foam is designed such thatthe patient may shift on the viscoelastic foam less than one inch, or upto approximately an inch, or in the range of approximately one inch toapproximately three inches. The airflow in or through the viscoelasticfoam is in the range of tenths of a cubic foot per minute to severalcubic feet per minute, such as, for example, approximately 0.1 or 0.3cubic foot per minute to approximately 1.0 or 3.0 cubic feet per minute,or is in the range of approximately 0.53 cubic feet per minute, plus orminus 0.3 cubic feet per minute. The thickness of the viscoelastic foamis in the range of from three-fourths of an inch to one inch, or toapproximately one inch, or to one and a half inches, or to three inchesor greater, which thickness is selected to minimize and/or preventbottoming out on the operating table of one or more of the portions ofthe body of a patient lying on the viscoelastic foam pad, depending onthe weight and/or size of the patient. The tensile strength (at 25percent deflection) of the viscoelastic foam is in the range of at leastapproximately 5 pounds per square inch (PSI) or approximately 8 PSI toapproximately 12 PSI or approximately 15 PSI, or is in the range ofapproximately 10 PSI. The tear strength (in a twenty inches per minutetest) of the viscoelastic foam is in the range of approximately one toapproximately two or three pounds of force per inch, or in the range ofapproximately 1.5 pounds of force per inch. The elongation (in a twentyinches per minute test) of the viscoelastic foam is in the range ofbetween 125 and 250 percent, or is in the range of approximately 172percent, plus or minus 25 percent. The nominal density of theviscoelastic foam is in a range of approximately 100 kilograms per cubicmeter, or is in the range of approximately 75 or 83 kilograms per cubicmeter to approximately 103 or 110 kilograms per cubic meter, such as,for example, 93.1 kilograms per cubic meter. The flammability of theviscoelastic foam should pass various tests by CAL, FMVSS and FAR, andthe viscoelastic foam should pass the European Union's Restriction ofHazardous Substances (EU RoHS) standards.

According to at least one possible embodiment, the viscoelastic foam padcan be of varying lengths, and can extend from either the feet, lowerlegs, thighs, or buttocks of a patient to either the shoulders, head, ortop of the head of a patient. According to at least one possibleembodiment, the viscoelastic foam pad or substantial portions thereofare pink in color, the straps for securing the patient to the pad arepurple in color, and the straps for securing the pad to the table orsurface are white.

As shown in FIG. 1, a Trendelenburg pad 102 may comprise fasteners 104extending beyond longitudinal sides of the Trendelenburg pad 102. Eachend of the fasteners 104 may comprise a hook and loop fastener, such asa Velcro® fastener, configured and disposed to attach the Trendelenburgpad 102 to operating table rails or other adjacent structures, dependingon the support structure on which the patient is positioned, which mayor may not be an operating bed. For example, each end of a fastener 104may comprise a loop portion 108 and a hook portion 106, extending beyondthe loop portion 108. Additionally, one or more portions of thefasteners 104 extending beyond the Trendelenburg pad 102 may comprise alabel 110 indicating the orientation that the Trendelenburg pad 102 isto have with an operating table. For example, the label 110 may state“this side up.”

In at least one possible embodiment of the present application, theTrendelenburg pad 102 may be a disposable pad and/or single-use pad.

FIG. 2 shows a bottom view of a Trendelenburg pad 102 comprisingfasteners 104 extending latitudinally therewith. A central portion 112of the fasteners 104 may be configured to be fastened with theTrendelenburg pad 102. For example, the central portion 112 may comprisehooks configured and disposed to fasten with loops on the Trendelenburgpad 102. The Trendelenburg pad 102 may be configured to fasten with twoor more fasteners 104. The fasteners may be Velcro®.

FIGS. 3A and 3B show a top view and a side view of a fastener 104respectively. A central portion 112 of fastener 104 may comprise loopson a side configured to fasten with hooks on a Trendelenburg pad 102 asshown in FIG. 2. A weld 115 may secure a hook portion 108 and a loopportion 106 to the central portion 112 wherein the ends of fastener 104comprises a hook portion 108 and a loop portion 106. It is to beunderstood that either portion 108 or 106 may comprise hooks and theother of 108 or 106 may comprise loops. A label 110 may be secured to anupper side of hook portion 108. An end of the hook portion 108 may befolded and welded at a weld point 111 to form a tab 109. Hooks 113 mayextend from a lower surface of the hook portion 108. Loops 107 mayextend from a lower surface of the loop portion 106.

FIG. 4 shows a use of Trendelenburg pad 102. For example, Trendelenburgpad 102 may be used by:

1. Placing a surgical operating table 120, having surgical operatingtable rails 124, in a Lithotomy Position.

2. Placing a longitudinal distal end of the Trendelenburg pad 102 on alongitudinal distal end of the surgical operating table 120.

3. Latitudinally centering the Trendelenburg pad 102 with the surgicaloperating table 120.

4. Positioning straps 104, extending from longitudinal edges of theTrendelenburg pad 102, down away from where a patient 128 will lie.

5. Attaching the straps 104 to the surgical operating table rails 124.

6. Laying a lift sheet 126 over the Trendelenburg pad 102.

7. Laying a patient 128 on the Trendelenburg pad 102 by positioning thepatient 128 so that the patient's shoulders do not extend past edges ofthe Trendelenburg pad 102.

8. Lifting the lift sheet 126 thereby lifting the patient 128 up and offthe Trendelenburg pad 102 to reposition the patient 128 as needed.

9. Positioning the patient's arms as needed.

10. Attaching body straps 130 around the patient and the surgicaloperating table.

11. Securing the patient's legs in stirrups 122.

12. Placing the surgical operating table in the Trendelenburg position.

In at least one possible embodiment of the present application, apatient may be disposed on a Trendelenburg pad 102 such that thepatient's skin contacts the Trendelenburg pad 102, for example that thepatient's skin contacts the Trendelenburg pad 102 in the patient'ssacrum and scapula areas of the body and held by the Trendelenburg pad102. The lift sheet 126 may be used to lift and reposition the patientwithout dragging the patient across the Trendelenburg pad.

Also shown in FIG. 4 are body straps 130. The body straps 130 maycomprise a hook strap 132 and a loop strap 134, such as a Velcro® strap.Each hook strap 132 and each loop strap 134 may comprise a clasp at oneend. A hook strap 132 may be secured to a operating table rail 124 bylooping therearound and extending through the clasp. A loop strap 134may be secured to the other operating table rail 124 by loopingtherearound and extending through the clasp, or secured by extending thehook strap 132 around or to some other portion of the operating table.The hook strap 132 and the loop strap 134 may be fastened about apatient 128, holding the patient 128 to the Trendelenburg pad 102. It isto be understood that body straps 130 are optional as the Trendelenburgpad 102 may provide adequate support of the patient 128 a on surgicaloperating table 120.

FIG. 5 shows a Trendelenburg pad 102 having an impression or residualcompression 130 of a patient therein. The Trendelenburg pad 102comprises viscoelastic foam which conforms to the patient's body andshapes itself to support the body. This shape minimizes pressure pointson the body and helps to hold the body on the operating table.

The holding quality or ability between the Trendelenburg Pad and apatient will be a combination of the coefficient of friction between thepatient and the viscoelastic foam and the holding ability of theimpression made by the patient in the viscoelastic foam, because theTrendelenburg pad is made of a viscoelastic foam in which an impressionis formed and held in the foam at least for a time after the patient ismoved from one position to another or from the operating table (see FIG.5). The equivalent total frictional characteristic, which includes thefriction due to the coefficient of friction and the friction orfriction-like force due to the viscoelastic foam deformation, may beequal to or in excess of one. That is to say, the normal, perpendicularforce onto the viscoelastic pad from the body of the patient andcomponent of the force of gravity on the patient parallel to the surfaceof the operating table at forty-five degrees are equal, which means thatthe equivalent total frictional characteristic will be equal to orgreater than the normal, perpendicular force. For an angle of forty-fivedegrees, the equivalent total frictional characteristic is one, which is[sin 45°/cos 45° ]. Stated more generally, the equivalent totalfrictional characteristic would be greater than the sine of the angle ofinclination from the horizontal over the cosine of the angle ofinclination from the horizontal. Since the angle can vary in one degreeor smaller increments, the range of values of the equivalent totalfrictional characteristic could vary between any of those angles so asto be at least or greater than the sine over cosine values of each ofthese angles of inclination at least within the range of greater thanzero degrees to forty-five degrees and also somewhat over forty-fivedegrees and even greater. The holding capabilities are a combination ofthe holding ability of the pad, the body straps, and the coefficient offriction of the pad with respect to the patient and the table, betweenthe pad and the sheet between the pad and the patient, and between thesheet and the patient, for all described angles.

FIG. 6 shows a Trendelenburg pad 102 of the present application securedto a surgical operating table 120 with fasteners 104. A patient 128 ispositioned on the Trendelenburg pad 102, and the surgical operatingtable 120 is in the Trendelenburg position. Also shown in FIG. 6 is anaspect of the Trendelenburg pad 102 wherein body straps 130 are notneeded to hold a patient 128 on the surgical operating table 120 in theTrendelenburg position.

FIG. 7 is a computer illustration of a person disposed on aTrendelenburg pad of one possible embodiment of the present application.The figure of the person is transparent or see-through, permitting aview of the impression on the Trendelenburg pad made by the figure ofthe person. The impression on the Trendelenburg pad may provide theprimary holding for holding a person on the operating table depending onthe angle of the patient on the table.

Referring now to FIG. 8, a block diagram of a robotic surgery system 200is illustrated to perform minimally invasive robotic surgical proceduresusing one or more robotic arms with strap drive. Robotic surgerygenerally involves the use of a robot manipulator that has multiplerobotic manipulator arms. One or more of the robotic manipulator armsoften support a surgical tool which may be articulated (such as jaws,scissors, graspers, needle holders, micro dissectors, staple appliers,tackers, suction/irrigation tools, clip appliers, or the like) ornon-articulated (such as cutting blades, cautery probes, irrigators,catheters, suction orifices, or the like). At least one of the roboticmanipulator arms (e.g., the center robotic manipulator arm 258B) is usedto support a stereo or three dimensional surgical image capture device210 such as a stereo endoscope (which may be any of a variety ofstructures such as a stereo laparoscope, arthroscope, hysteroscope, orthe like), or, optionally, some other stereo imaging modality (such asultrasound, fluoroscopy, magnetic resonance imaging, or the like).Robotic surgery may be used to perform a wide variety of surgicalprocedures, including but not limited to open surgery, neurosurgicalprocedures (such as stereotaxy), endoscopic procedures (such aslaparoscopy, arthroscopy, thoracoscopy), and the like.

A user or operator O (generally a surgeon) performs a minimally invasivesurgical procedure on patient P by manipulating control input devices260 at a master control console 250. A computer 251 of the console 250directs movement of robotically controlled endoscopic surgicalinstruments 201A-201C by means of one or more control cables 259,effecting movement of the instruments using a robotic patient-sidesystem 252 (also referred to as a patient-side cart). The roboticpatient-side system 252 has one or more robotic arms 258. In onepossible embodiment of the Da Vinci Surgical System, the one or morerobotic arms 258 have a strap drive system. Typically, the roboticpatient-side system 252 includes at least three robotic manipulator arms258A-258C supported by linkages 256, 256′, with a central robotic arm258B supporting an endoscopic camera 201B and the robotic arms 258A,258C to left and right of center supporting tissue manipulation tools201A and 201C.

Generally, the robotic patient-side system 252 includes a positioningportion and a driven portion. The positioning portion of the roboticpatient-side system 252 remains in a fixed configuration during surgerywhile manipulating tissue. The driven portion of the roboticpatient-side system 252 is actively articulated under the direction ofthe operator O generating control signals at the surgeon's console 250during surgery. The actively driven portion of the robotic patient-sidesystem 252 is generally referred to herein as the robotic arms oralternatively to robotic surgical manipulators. The positioning portionof the robotic patient-side system 252 that is in a fixed configurationduring surgery may be referred to as “set up arms” 256, 256′ withpositioning linkage and/or “set-up joints” (SUJ). In an alternateembodiment of the Da Vinci Surgical System, the robotic patient-sidesystem 252 may be replaced by set up arms that couple at one end to leftand right sides of the operating table T. The three robotic manipulatorarms 258A-258C may then be coupled to the opposite end of the set-uparms to ground to the table T.

For convenience in terminology, manipulators such as robotic surgicalarms 258A and 258C actuating the tissue affecting surgical tools 201Aand 201C are generally referred to herein as a PSM (patient-sidemanipulators), and a robotic surgical arm 258B controlling an imagecapture or data acquisition device, such as the endoscopic camera 201B,is generally referred to herein as a ECM (endoscope-camera manipulator),it being noted that such telesurgical robotic manipulators mayoptionally actuate, maneuver and control a wide variety of instruments,tools and devices useful in surgery. The surgical tools 201A, 201C andendoscopic camera 201B may be generally referred to herein as tools orinstruments 201.

An assistant A may assist in pre-positioning of the robotic patient-sidesystem 252 relative to patient P as well as swapping tools orinstruments 201 for alternative tool structures, and the like, whileviewing the internal surgical site via an assistant's display 254. Withthe embodiments of the Da Vinci Surgical System, the assistant A mayalso swap in and out the robotic surgical arms 258A and 258C, as well asthe robotic surgical arm 258B, in case one is defective or failing. Inother cases, a robotic surgical arm may be swapped out for maintenance,adjustments, or cleaning and then swapped back in by one or more servicepersons.

Referring now to FIG. 9, a perspective view of the robotic patient-sidesystem 252 is illustrated. The robotic patient-side system 252 may haveone or more robotic surgical arms (a.k.a., robotic surgicalmanipulators) 258A-258C with a strap drive system. The robotic arms258A, 258C are for coupling to robotic surgical tools 201A, 201C. Therobotic arm 258B is for coupling to an endoscopic camera 201B.Generally, the surgical robotic arms 258A-258C may be referred to as asurgical robotic arm or a robotic surgical arm 258.

The robotic patient-side system 252 further includes a base 302 fromwhich the robotic surgical instruments 201 may be supported. In at leastone possible embodiment of the Da Vinci Surgical System, the roboticsurgical instruments 201 are each supported by the positioning linkage256 and the surgical robotic arms 258. The linkage structures mayoptionally be covered by protective covers or not to minimize theinertia that is manipulated by the servomechanism and the overall weightof robotic patient-side system 252.

The robotic patient-side system 252 generally has dimensions suitablefor transporting between operating rooms. It typically can fit throughstandard operating room doors and onto standard hospital elevators. Therobotic patient-side system 252 may have a weight and a wheel (or othertransportation) system that allows the cart to be positioned adjacent toan operating table by a single attendant. The robotic patient-sidesystem 252 may be sufficiently stable during transport to avoid tippingand to easily withstand overturning moments that may be imposed at theends of the robotic arms during use.

FIG. 10 shows an example of a robotic surgery system 10, in which atleast one possible embodiment of the Trendelenburg pad could beutilized. In robotic surgery, the consistency of location of the patientis paramount because a shift in position may interfere with the relativepositioning of the instruments used in surgery. Due to the ability ofthe Trendelenburg pad to hold or assist in holding a patient in adesired position, the Trendelenburg pad could be used in roboticsurgery. The system 10 may be used to perform a procedure on a patient12 that is typically lying on an operating table 14. Mounted to theoperating table 14 is a first articulate arm 16, a second articulate arm18 and a third articulate arm 20. The articulate arms 16-20 are mountedto the table so that the arms are in a plane proximate the patient.

The articulate arms 16, 18 and 20 may each comprise a base housing 25and a robotic arm assembly 26 extending from the base housing 25.Surgical instruments 22 and 24 may be removably coupled at the end ofeach robotic arm assembly 26 of the first and second articulate arms 16,18. Each of the instruments 22, 24 may be coupled to a correspondingrobotic arm assembly 26.

The third articulate arm 20 may additionally comprise a base housing 25and a robotic arm assembly 26, and has a first endoscope 28 that isattached to the robotic arm assembly 26. The base housing 25 and roboticarm assemblies 26 of each of the articulate arms 16, 18, and 20 aresubstantially similar. Additionally, a fourth robotic arm 29 may beincluded in the system 10. The fourth arm 29 may hold a second endoscope31.

The instruments 22, 24 and endoscope 28 may be inserted throughincisions cut into and through the skin of the patient 12. The firstendoscope 28 may comprise a camera 30 that may be coupled to a monitor32. The monitor 32 may be configured to display images of the internalorgans of the patient 12. Additionally, the second endoscope 31 may beinserted through a corresponding incision made in the patient's skin.The second endoscope 31 may be used to provide a wide field of view asdepicted in FIG. 10. The second endoscope 31 may be mounted to thefourth robotic arm 29 and may be coupled to a second monitor 33.

Each robotic arm assembly 26 may comprise a base motor 34 which movesthe arm assembly 26 in a linear fashion, relative to the base housing25, as indicated by arrow Q. Each robotic arm assembly 26 may alsocomprise a first rotary motor 36 and a second rotary motor 38. Each ofthe robotic arm assemblies 26 may also comprise a pair of passive joints40 and 42. The passive joints 40, 42 may be disposed orthogonal to eachother to provide pivotal movement of the instruments 22, 24 or theendoscopes 28, 31 attached to a corresponding robotic arm assembly 26.The joint angle may be controlled to a particular value using a feedbackcontrol loop. The robotic arm assemblies 26 may also comprise a couplingmechanism 45 to couple the instruments 22 and 24, or endoscope 28, 31thereto. Additionally, each of the robotic arm assemblies 26 maycomprise a motor driven worm gear 44 being configured to rotate theinstrument 22, 24 or endoscope 28, 31 attached thereto about itslongitudinal axis.

The first, second, and third articulate arms 16, 18, 20, as well as thefourth arm 29, may be coupled to a controller 46 which may control themovement of the arms. The arms may be coupled to the controller 46 viawiring, cabling, or via a transmitter/receiver system such that controlsignals may be passed from the controller 46 to each of the articulate.Each arm 16, 18, 20 and 29 may be electrically connected to thecontroller 46 via electrical cabling 47.

The controller 46 may be connected to an input device 48 such as a footpedal, hand controller, or voice recognition unit, to control theposition of the endoscope 28 or the second endoscope. To effectuatevoice recognition, a microphone 37 is included in the system 10. Thecontroller 46 receives the input signals from the input device 48 andmoves the endoscope 28 and robotic arm assembly 26 of the thirdarticulate arm 20 in accordance with the input commands of the surgeon.

The movement and positioning of instruments 22, 24 attached to the firstand second articulate arms 16 and 18 is controlled by a surgeon at apair of master handles 50 and 52. Additionally, a switch 51 may beincluded in the system 10. The switch 51 may be used by the surgeon toallow positioning of the fourth arm 29. The handles 50 and 52 may bemounted to a portable cabinet 54. A television monitor 56 may be placedonto the cabinet 54 and coupled to the endoscope 28 so that the surgeoncan readily view the internal organs of the patient 12. To accommodate aseated position, a chair 57 may be provided with the system.

FIG. 11 is a representation of a table inclined at a forty-five degreeangle. W is the weight of a patient. The normal force perpendicular tothe surface of the operating table is 0.707 W. The force along the tableis 0.707 W. The equivalent coefficient of friction including the actualcoefficient of friction and holding ability of the Trendelenburg pad andthe fasteners 130 of the present application to hold a patient is 1.00.

The positioning arrangement and arrangements in the present applicationcould be used in gynecological procedures, colorectal procedures,urological procedures, laparoscopic procedures, and robotic proceduresto name some procedures to use this pad in the Trendelenburg or thereverse Trendelenburg position. The positioning arrangement andarrangements, and embodiments of the Trendelenburg pad and kit, in thepresent application could also be used in all types of medicalprocedures in which it may be desirable to place a patient in a secureand/or reduced pressure point and/or comfortable position, which medicalprocedures include surgical procedures and non-surgical procedures, suchas non-surgical examinations and/or treatments.

The viscoelastic foam of the present application may be a polyurethanefoam made by mixing polyhydroxy polyol with toluene di-isocyanate orother and different methods as are known in the art. For example,Toluene di-isocyanate may be used in combination with polyester polyolsand polyether to make viscoelastic foam.

In at least one other aspect of the present disclosure, theTrendelenburg pad 102 is about twenty inches wide, about thirty incheslong, and about one inch thick. In one possible embodiment of thepresent application, the thickness of the pad may be in the range ofapproximately three-quarters of an inch to approximately one andone-half inches. In that range, the thickness may increase or decreasein increments of 1/32 of an inch. In one possible embodiment of thepresent application, the width of the pad may be in range ofapproximately twenty inches to approximately twenty-eight inches. Inthat range, the width may increase or decrease in increments ofone-fourth of an inch or less. In one possible embodiment of the presentapplication, the length of the pad may be in the range of approximatelythirty inches to approximately forty inches. In that range, the lengthmay increase or decrease in increments of one-fourth of an inch or less.The fasteners 104 may be Velcro® straps and may be about two incheswide. The fasteners 104 may be secured to the Trendelenburg pad 102 bywelding, adhesive, hook and loop fastening, or by other means as isknown in the art.

An example of a robotic surgery system, such as the Da Vinci SurgicalSystem, is made by Intuitive Surgical, Inc., located at 1266 Kifer Road#101, Sunnyvale, Calif. 94086.

U.S. Pat. No. 8,066,524, having the title “SURGICAL SYSTEM WITHELECTRO-MECHANICAL INTERFACES TO MOUNT ROBOTIC SURGICAL ARMS,” issued onNov. 29, 2011, is hereby incorporated by reference as if set forth inits entirety herein except for the exceptions indicated herein.

Words relating to the opinions and judgments of the author of allpatents, patent applications, patent publications, and other documentscited herein and not directly relating to the technical details of thedescription of the embodiments therein are not incorporated byreference.

The words all, always, absolutely, consistently, preferably, guarantee,particularly, constantly, ensure, necessarily, immediately, endlessly,avoid, exactly, continually, expediently, ideal, need, must, only,perpetual, precise, perfect, require, requisite, simultaneous, total,unavoidable, and unnecessary, or words substantially equivalent to theabove-mentioned words in this sentence, when not used to describetechnical features of one or more embodiments of the patents, patentapplications, patent publications, and other documents, are notconsidered to be incorporated by reference herein for any of thepatents, patent applications, patent publications, and other documentscited herein.

One feature or aspect of an embodiment is believed at the time of thefiling of this patent application to possibly reside broadly in a methodof minimizing injuries caused by pressure on portions of a body of apatient in the Trendelenburg position on a surgical operating table, andminimizing unwanted movement of a patient in the Trendelenburg positionon a surgical operating table by securing a patient to the surgicaloperating table, and also minimizing contamination in an operating room,by using a single-use Trendelenburg patient support system comprising: alift sheet configured to lift and position a patient on a surgicaloperating table, body straps configured to hold a patient down on asurgical operating table, a single-use, viscoelastic Trendelenburg padcomprising a rectangular shape and viscoelastic polyurethane, andsecuring straps welded to said single-use, viscoelastic Trendelenburgpad, which said securing straps are configured to secure saidsingle-use, viscoelastic Trendelenburg pad to rails of a surgicaloperating table, said method comprising the steps of: A) placing alongitudinal edge of said single-use, viscoelastic Trendelenburg padadjacent and in alignment with a longitudinal edge of a surgicaloperating table having surgical operating table rails; B) placing alatitudinal edge of said single-use, viscoelastic Trendelenburg padadjacent and in alignment with a latitudinal edge of said surgicaloperating table, and thus positioning said single-use, viscoelasticTrendelenburg pad in a position on said surgical operating table wherethe body of a patient will be lying; C) positioning said securingstraps, extending from longitudinal edges of said single-use,viscoelastic Trendelenburg pad, to extend down and away from saidsingle-use, viscoelastic Trendelenburg pad; D) attaching said securingstraps to said surgical operating table rails; E) laying said lift sheetover said single-use, viscoelastic Trendelenburg pad; F) laying apatient in a supine position on said lift sheet and said single-use,viscoelastic Trendelenburg pad by positioning said patient so that theshoulders of said patient do not extend past edges of said single-use,viscoelastic Trendelenburg pad, and thereby deforming said single-use,viscoelastic Trendelenburg pad, which said single-use, viscoelasticTrendelenburg pad comprises: sufficient thickness and viscosity tosufficiently cushion the body of said patient to minimize and/or preventbottoming out on said medical procedure table of one or more of theportions of the body of said patient during positioning of said patientand during a surgical procedure, and to minimize injuries from pressureduring a surgical procedure performed while a patient is in lithotomyand Trendelenburg positions, and sufficient compliance to conform to asubstantial portion of the body of said patient; G) lifting said liftsheet and thereby lifting said patient up and off said single-use,viscoelastic Trendelenburg pad to reposition said patient as or ifneeded; H) positioning the arms of said patient as or if needed; l)attaching said body straps around said patient and said surgicaloperating table; J) positioning the legs of said patient in a lithotomyposition; K) adjusting the angle of inclination of said surgicaloperating table to orient said patient at an angle in a Trendelenburgposition in which the head of said patient is disposed below the body ofsaid patient, or in which the head of said patient is disposed above thebody of said patient, or in which the right side of a patient isdisposed above the left side or vice versa, or a combination of any ofthese positions; and L) assisting in substantially holding the body ofsaid patient on said surgical operating table in said lithotomy andTrendelenburg positions using said single-use, viscoelasticTrendelenburg pad, which said single-use, viscoelastic Trendelenburg padcomprises: sufficient thinness to stabilize said patient on saidsurgical operating table upon said patient being in said lithotomy andTrendelenburg positions, and sufficient thickness and sufficientcompliance to permit formation of a cavity in said single-use,viscoelastic Trendelenburg pad of a depth sufficient to assist inholding said patient on said surgical operating table and/or minimizingundesired movement of the body of said patient on said surgicaloperating table during a surgical procedure performed while said patientis in said lithotomy and Trendelenburg positions.

Another feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in themethod, wherein: said single-use Trendelenburg patient support systemcomprises a kit; said step D) comprises using securing straps comprisinga central portion, attached to a lower side of said single-use,viscoelastic Trendelenburg pad, and fastener ends, each comprising ahook and loop fastener; said single-use, viscoelastic Trendelenburg padhas a thickness in the range of from three-fourths of an inch to threeinches or greater; and said single-use, viscoelastic Trendelenburg padcomprises a viscoelastic polyurethane foam having: a ball reboundsufficiently small to minimize rebound of said patient during anoperation; a compression set sufficiently small to minimize discomfortof and injury to said patient on said surgical operating table; an airflow sufficient to provide substantial air flow about said patient tominimize injury to said patient and maintain a patient in a useableTrendelenburg position; an indentation force deflection sufficient toprovide a securing hold on said patient; a tensile strength sufficientto minimize tearing of said single-use, viscoelastic Trendelenburg pad;a coefficient of static friction sufficient to assist in minimizingmovement of said single-use, viscoelastic Trendelenburg pad on saidsurgical operating table when said patient is on said surgical operatingtable; and a density configured to provide said ball rebound, saidcompression set, said air flow, said indentation force deflection, saidtensile strength, and said coefficient of static friction.

Yet another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe method, wherein: said single-use, viscoelastic Trendelenburg pad hasa thickness of approximately one inch; said ball rebound is in the rangeof approximately 0.1 percent to approximately 1.9 percent; saidcompression set, for a 25 percent compression, is less than 0.3 percent;said air flow is in the range of 0.3 to 1.0 cubic foot per minute; saidindentation force deflection is in the range of approximately 10 toapproximately 15 pounds; said tensile strength is in the range ofapproximately 8 pounds per square inch to approximately 12 pounds persquare inch; said coefficient of static friction is in the range of 0.2to 1.0; and said density is in the range of approximately 83 kilogramsper cubic meter to approximately 103 kilograms per cubic meter.

Still another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly in asingle-use Trendelenburg patient support system for performing themethod, said single-use Trendelenburg patient support system comprising:a lift sheet configured to lift and position a patient on a surgicaloperating table; body straps configured to hold a patient down on asurgical operating table; a single-use, viscoelastic Trendelenburg padcomprising a rectangular shape and viscoelastic polyurethane; securingstraps welded to said single-use, viscoelastic Trendelenburg pad; saidsecuring straps being configured to secure said single-use, viscoelasticTrendelenburg pad to rails of a surgical operating table; saidsingle-use, viscoelastic Trendelenburg pad comprising: sufficientthickness and viscosity to sufficiently cushion the body of a patient tominimize and/or prevent bottoming out on said medical procedure table ofone or more of the portions of the body of a patient during positioningof a patient and during a surgical procedure, and to minimize injuriesfrom pressure during a surgical procedure; sufficient compliance toconform to a substantial portion of the body of a patient; sufficientthinness to stabilize a patient on said surgical operating table upon apatient being in lithotomy and Trendelenburg positions; and sufficientthickness and sufficient compliance to permit formation of a cavity insaid single-use, viscoelastic Trendelenburg pad of a depth sufficient toassist in holding a patient on said surgical operating table and/orminimizing undesired movement of the body of a patient on said surgicaloperating table during a surgical procedure performed while a patient isin lithotomy and Trendelenburg positions.

A further feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thesingle-use Trendelenburg patient support system, wherein: saidsingle-use Trendelenburg patient support system comprises a kit; saidbody straps comprise hook and loop fasteners; said securing straps eachcomprise a central portion, attached to a lower side of said single-use,viscoelastic Trendelenburg pad, and fastener ends, each comprising ahook and loop fastener; said single-use, viscoelastic Trendelenburg padhas a thickness of approximately one inch; and said single-use,viscoelastic Trendelenburg pad comprises a viscoelastic polyurethanehaving: a ball rebound in the range of approximately 0.1 percent toapproximately 1.9 percent; a compression set, for a 25 percentcompression, of less than 0.3 percent; an air flow in the range of 0.3to 1.0 cubic foot per minute; an indentation force deflection in therange of approximately 10 to approximately 15 pounds; a tensile strengthin the range of approximately 8 pounds per square inch to approximately12 pounds per square inch; a coefficient of static friction in the rangeof 0.2 to 1.0; and a density in the range of approximately 83 kilogramsper cubic meter to approximately 103 kilograms per cubic meter.

Another feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in amethod of minimizing injuries caused by pressure on portions of a bodyof a patient and minimizing unwanted movement of a patient upon securinga patient to a medical procedure table, such as a surgical operatingtable or a patient examination table, and upon placing said medicalprocedure table in an inclined position, using a patient support systemcomprising a viscoelastic pad and securing straps, said methodcomprising the steps of: A) positioning said viscoelastic pad in aposition on said medical procedure table where the body of a patientwill be lying; B) attaching said securing straps, connected to saidviscoelastic pad, to said medical procedure table; C) positioning apatient on said viscoelastic pad and thereby deforming said viscoelasticpad, which said viscoelastic pad comprises: sufficient thickness andviscosity to sufficiently cushion the body of said patient to minimizeand/or prevent bottoming out on said medical procedure table of one ormore of the portions of the body of said patient during positioning ofsaid patient and during a medical procedure, and to minimize injuriesfrom pressure during a medical procedure, and sufficient compliance toconform to a substantial portion of the body of said patient; D)adjusting the angle of inclination of said medical procedure table toorient said patient at an angle in an inclined position, in which thehead of said patient is disposed below the body of said patient, or inwhich the head of said patient is disposed above the body of saidpatient, or in which the right side of a patient is disposed above theleft side or vice versa, or a combination of any of these positions; andE) assisting in substantially holding the body of said patient on saidmedical procedure table using said viscoelastic pad, of which saidviscoelastic pad comprises: sufficient thinness to stabilize saidpatient on said medical procedure table upon said patient being in saidinclined position, and sufficient thickness and sufficient compliance topermit formation of a cavity in said viscoelastic pad of a depthsufficient to assist in holding a patient on a medical procedure tableand/or minimizing undesired movement of the body of a patient on amedical procedure table during a medical procedure performed while apatient is in an inclined position.

Yet another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe method, wherein: said patient support system further comprises atleast one body strap; said patient support system comprises a kit; saidmethod further comprises attaching said at least one body strap aroundsaid patient and said medical procedure table between steps C) and D);said step B) comprises using securing straps comprising a centralportion, attached to a lower side of said viscoelastic pad, and fastenerends, each comprising a hook and loop fastener; said step D) comprisesadjusting the angle of inclination of said medical procedure table toorient said patient in a Trendelenburg position; said viscoelastic padhas a thickness in the range of from three-fourths of an inch to threeinches or greater; and said viscoelastic pad comprises a viscoelasticpolyurethane foam having: a ball rebound sufficiently small to minimizerebound of said patient during an operation; a compression setsufficiently small to minimize discomfort of and injury to said patienton said medical procedure table; an air flow sufficient to providesubstantial air flow about said patient to minimize injury to saidpatient and maintain a patient in an inclined position; an indentationforce deflection sufficient to provide a securing hold on said patient;a tensile strength sufficient to minimize tearing of said viscoelasticpad; a coefficient of static friction sufficient to assist in minimizingmovement of said viscoelastic pad on said medical procedure table whensaid patient is on said medical procedure table; and a densityconfigured to provide said ball rebound, said compression set, said airflow, said indentation force deflection, said tensile strength, and saidcoefficient of static friction.

Still another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly in apatient support system for performing the method, said patient supportsystem comprising: a viscoelastic pad; securing straps connected to saidviscoelastic pad; said securing straps being configured to secure saidviscoelastic pad to a medical procedure table; said viscoelastic padcomprising: sufficient thickness and viscosity to sufficiently cushionthe body of a patient to minimize and/or prevent bottoming out on amedical procedure table of one or more of the portions of the body of apatient during positioning of a patient and during a medical procedure,and to minimize injuries from pressure during a medical procedure;sufficient compliance to conform to a substantial portion of the body ofa patient; sufficient thinness to stabilize a patient on a medicalprocedure table upon a patient being in an inclined position; sufficientthinness to stabilize a patient on a medical procedure table upon apatient being in an inclined position, and sufficient thickness andsufficient compliance to permit formation of a cavity in saidviscoelastic pad of a depth sufficient to assist in holding a patient ona medical procedure table and/or minimizing undesired movement of thebody of a patient on a medical procedure table during a medicalprocedure performed while a patient is in an inclined position.

A further feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thepatient support system, wherein: said patient support system furthercomprises at least one body strap configured to hold a patient down on amedical procedure table while a patient is in a Trendelenburg position;said patient support system comprises a kit; said at least one bodystrap comprises hook and loop fasteners; said securing straps eachcomprise a central portion, attached to a lower side of saidviscoelastic pad, and fastener ends, each comprising a hook and loopfastener; said viscoelastic pad has a thickness in the range of fromthree-fourths of an inch to three inches or greater; and saidviscoelastic pad comprises a viscoelastic polyurethane foam having: aball rebound in the range of approximately 0.1 percent to approximately5 percent; a compression set, for a 25 percent compression, of less thanone percent; a air flow in the range of 0.1 to 3.0 cubic foot perminute; a indentation force deflection in the range of approximately 7to approximately 18 pounds; a tensile strength in the range ofapproximately 5 pounds per square inch to approximately 15 pounds persquare inch; a coefficient of static friction is at least 0.2; and adensity in the range of approximately 75 kilograms per cubic meter toapproximately 110 kilograms per cubic meter.

Another feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in apatient support arrangement configured to support and assist in holdinga patient on an inclined medical procedure table, said patient supportarrangement comprising: a pad comprising a thickness and a viscositysufficient to cushion the body of a patient to minimize injuries frompressure during a medical procedure, and to minimize and/or preventbottoming out on a medical procedure table of one or more of theportions of the body of a patient both during positioning of a patientand during a medical procedure; said pad comprising a compliancesufficient to permit said pad to conform to a substantial portion of thebody of a patient; said thickness being sufficiently small to stabilizea patient on a medical procedure table upon a patient being in aninclined position; and said thickness and said compliance beingsufficient to permit deformation of said pad to a depth sufficient toassist in holding a patient on a medical procedure table, and to assistin minimizing undesired movement of the body of a patient on a medicalprocedure table, during a medical procedure performed while a patient isin an inclined position.

Yet another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe patient support arrangement, wherein said pad comprises a rebound,such as ball rebound, being sufficiently small to minimize undesirablemovement of a patient during a medical procedure.

Still another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe patient support arrangement, wherein said ball rebound is in therange of approximately 0.1 percent to approximately 5 percent.

A further feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thepatient support arrangement, wherein said ball rebound is in the rangeof approximately 0.1 percent to approximately 1.9 percent.

One feature or aspect of an embodiment is believed at the time of thefiling of this patent application to possibly reside broadly in thepatient support arrangement, wherein said pad comprises a compressionset being sufficiently small to minimize discomfort of and injury to apatient on a medical procedure table.

Another feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thepatient support arrangement, wherein said compression set, for a 25percent compression, is less than one percent.

Yet another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe patient support arrangement, wherein said compression set, for a 25percent compression, is less than 0.3 percent.

Still another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe patient support arrangement, wherein said pad comprises anindentation force deflection sufficient to provide a securing hold on apatient.

A further feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thepatient support arrangement, wherein said indentation force deflectionis in the range of approximately 7 to approximately 18 pounds.

Another feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thepatient support arrangement, wherein said indentation force deflectionis in the range of approximately 10 to approximately 15 pounds.

Yet another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe patient support arrangement, wherein said pad comprises: acompression set being sufficiently small to minimize discomfort of andinjury to a patient on a medical procedure table; and an indentationforce deflection sufficient to provide a securing hold on a patient.

Still another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe patient support arrangement, wherein: said pad has a thickness inthe range of from three-fourths of an inch to three inches or greater;and said pad comprises: an air flow sufficient to provide substantialair flow about a patient to minimize injury to a patient and maintain apatient in an inclined position; a tensile strength sufficient tominimize tearing of said pad; a coefficient of static frictionsufficient to assist in minimizing movement of said pad on a medicalprocedure table when a patient is on a medical procedure table; and adensity configured to provide said ball rebound, said compression set,said air flow, said indentation force deflection, said tensile strength,and said coefficient of static friction.

A further feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thepatient support arrangement, wherein: said ball rebound is in the rangeof approximately 0.1 percent to approximately 5 percent; saidcompression set, for a 25 percent compression, is less than one percent;said air flow is in the range of 0.1 to 3.0 cubic foot per minute; saidindentation force deflection is in the range of approximately 7 toapproximately 18 pounds; said tensile strength is in the range ofapproximately 5 pounds per square inch to approximately 15 pounds persquare inch; said coefficient of static friction is at least 0.2; andsaid density is in the range of approximately 75 kilograms per cubicmeter to approximately 110 kilograms per cubic meter.

Another feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thepatient support arrangement, wherein: said ball rebound is in the rangeof approximately 0.1 percent to approximately 1.9 percent; saidcompression set, for a 25 percent compression, is less than 0.3 percent;said air flow is in the range of 0.3 to 1.0 cubic foot per minute; saidindentation force deflection is in the range of approximately 10 toapproximately 15 pounds; said tensile strength is in the range ofapproximately 8 pounds per square inch to approximately 12 pounds persquare inch; said coefficient of static friction is in the range of 0.2to 1.0; and said density is in the range of approximately 83 kilogramsper cubic meter to approximately 103 kilograms per cubic meter.

Yet another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe patient support arrangement, wherein at least one of a)-g): a) saidball rebound is in the range of approximately 0.1 percent toapproximately 5 percent; b) said compression set, for a 25 percentcompression, is less than one percent; c) said air flow is in the rangeof 0.1 to 3.0 cubic foot per minute; d) said indentation forcedeflection is in the range of approximately 7 to approximately 18pounds; e) said tensile strength is in the range of approximately 5pounds per square inch to approximately 15 pounds per square inch; f)said coefficient of static friction is at least 0.2; and g) said densityis in the range of approximately 75 kilograms per cubic meter toapproximately 110 kilograms per cubic meter.

Still another feature or aspect of an embodiment is believed at the timeof the filing of this patent application to possibly reside broadly inthe patient support arrangement, wherein at least one of h)-n): h) saidball rebound is in the range of approximately 0.1 percent toapproximately 1.9 percent; i) said compression set, for a 25 percentcompression, is less than 0.3 percent; j) said air flow is in the rangeof 0.3 to 1.0 cubic foot per minute; k) said indentation forcedeflection is in the range of approximately 10 to approximately 15pounds; l) said tensile strength is in the range of approximately 8pounds per square inch to approximately 12 pounds per square inch; m)said coefficient of static friction is in the range of 0.2 to 1.0; andn) said density is in the range of approximately 83 kilograms per cubicmeter to approximately 103 kilograms per cubic meter.

A further feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thepatient support arrangement, wherein: said pad comprises a viscoelasticmaterial; said patient support arrangement further comprises securingstraps attached to said pad and at least one body strap; said securingstraps are configured to secure said pad to a medical procedure table;said securing straps each comprise a central portion, attached to alower side of said pad, and fastener ends, each comprising a hook andloop fastener; said at least one body strap is configured to hold apatient down on a medical procedure table while a patient is in aTrendelenburg position; and said patient support arrangement comprises akit.

One feature or aspect of an embodiment is believed at the time of thefiling of this patent application to possibly reside broadly in apatient support arrangement configured to support and assist in holdinga patient in a Trendelenburg position on an inclined medical proceduretable, in which the head of the patient is disposed below the body ofthe patient, or in which the head of the patient is disposed above thebody of the patient, or in which the right side of the patient isdisposed above the left side or vice versa, or a combination of any ofthese positions, said patient support arrangement comprising: a padcomprising a viscoelastic polyurethane foam; said pad comprising athickness and softness sufficient to permit deformation of said pad to adepth sufficient to assist in holding a patient on a medical proceduretable during a medical procedure performed while a patient is in aTrendelenburg position; and said pad being configured to recover from adeformation at a rate in a range sufficient to maintain support andminimize disruptive movement of at least a portion of a body of apatient on a medical procedure table during a medical procedureperformed while a patient is in a Trendelenburg position.

Another feature or aspect of an embodiment is believed at the time ofthe filing of this patent application to possibly reside broadly in thepatient support arrangement, wherein said rate of recovery of said padis insufficient to assist in causing disruptive movement of at least aportion of a body of a patient.

The appended drawings in their entirety, including all dimensions,proportions and/or shapes in at least one embodiment of the invention,are accurate and are hereby included by reference into thisspecification.

The embodiments of the invention described herein above in the contextof the preferred embodiments are not to be taken as limiting theembodiments of the invention to all of the provided details thereof,since modifications and variations thereof may be made without departingfrom the spirit and scope of the embodiments of the invention.

What is claimed is:
 1. A surgical patient single use, open cell foamsupport pad comprising a viscoelastic memory foam which has acoefficient of friction between said viscoelastic memory foam and asurface of a surgical procedure table configured to hold said pad on asurgical procedure table, which surgical patient single use, open cellfoam support pad comprises viscoelastic memory foam which is deformableso as to conform to a body of a patient, and which thereby assists inholding a patient in an inclined, Trendelenburg, position on an inclinedsurgical procedure table, and prevents or minimizes bottoming out on asurgical procedure table of a portion of a body of a patient to reduceinjury caused by pressure to a patient during a surgical procedure,where an inclined, Trendelenburg, position includes an orientation inwhich a head of a patient is disposed either a) below or b) above a bodyof a patient or c) a right side of a patient is disposed higher than aleft side of a patient, or d) a left side of a patient is disposedhigher than a right side of a patient, or e) a combination of a), b),c), and d); said surgical patient single use, open cell foam support padfurther comprising: a flat top surface and a flat bottom surface; asingle layer of viscoelastic memory foam; said viscoelastic memory foamis uncovered on its top and bottom; said single layer of saidviscoelastic memory foam extends all the way through said surgicalpatient single use, open cell foam support pad from a patient's skin toa surface of a surgical procedure table between the flat top surface andthe flat bottom surface of said surgical patient single use, open cellfoam support pad; said viscoelastic memory foam comprising a coefficientof static friction in the range of 0.2 to 1.0 and said coefficient ofstatic friction being at a value in said range sufficient to assist inminimizing movement of said surgical patient single use, open cell foamsupport pad on a surgical procedure table upon a patient being on asurgical procedure table; sufficient thickness and viscosity tosufficiently cushion a body of a patient to: minimize bottoming out orprevent bottoming out, on a surgical procedure table, of one or more ofportions of a body of a patient during positioning of a patient andduring a surgical procedure, and to minimize injuries from pressure on apatient during a surgical procedure; sufficient compliance to conform toa substantial portion of a body of a patient; sufficient thinness tostabilize a patient on a surgical procedure table; and said sufficientthickness and said sufficient compliance being configured to permitformation of a cavity in said surgical patient single use, open cellfoam support pad of a depth sufficient to at least one of: assist inholding a patient on a surgical procedure table, and assist inminimizing undesired movement of a body of a patient on a surgicalprocedure table, during a surgical procedure performed while a patientis in an surgical position; said surgical patient single use, open cellfoam support pad being configured to generate a sufficient staticfrictional force on skin of a patient on said surgical patient singleuse, open cell foam support pad to stabilize a patient on said surgicalpatient single use, open cell foam support pad; said surgical patientsingle use, open cell foam support pad is configured to generate afriction or friction-like force due to formation of a cavity in saidsurgical patient single use, open cell foam support pad, and which forcegenerated by said coefficient of static friction both together beingsufficient to hold a body of a patient substantially static on asurgical procedure table; wherein a holding quality or ability betweensaid surgical patient single use, open cell foam support pad and apatient is a combination of the coefficient of friction between apatient and said viscoelastic memory foam and the holding ability of theimpression made by a patient in said viscoelastic memory foam; saidholding quality or ability comprising an equivalent total frictionalcharacteristic including the friction due to the coefficient of frictionand the friction or friction-like force due to the viscoelastic memoryfoam deformation; said viscoelastic memory foam pad comprises aviscoelastic foam in which an impression is formed and held in the foamat least for a time after a patient is moved from one position toanother or from a surgical procedure table; said open cell foam alsoprovides an air flow sufficient to provide substantial air flow about apatient; and wherein said air flow of said open cell foam is in therange of one of i) and ii), wherein i) and ii) are: i) 0.1 to 3.0 cubicfoot per minute; and ii) 0.3 to 1.0 cubic foot per minute.
 2. A singleuse pad patient support system configured to minimize injuries caused bypressure on portions of a body of a patient and minimize unwantedmovement of a patient upon a patient being positioned on a surgicalprocedure table, such as a surgical operating table or a patientexamination table, said single use memory pad patient support systemcomprising a pad; said pad comprising: a viscoelastic, polyurethane opencell foam comprising a coefficient of static friction in the range of0.2 to 1.0 and said coefficient of static friction being at a value insaid range sufficient to assist in minimizing movement of said pad on asurgical procedure table upon a patient being on a surgical proceduretable; sufficient thickness and viscosity to sufficiently cushion a bodyof a patient to: minimize bottoming out or prevent bottoming out, on asurgical procedure table, of one or more of portions of a body of apatient during positioning of a patient and during a surgical procedure,and to minimize injuries from pressure on a patient during a surgicalprocedure; and sufficient compliance to conform to a substantial portionof a body of a patient; sufficient thinness to stabilize a patient on asurgical procedure table; and said sufficient thickness and saidsufficient compliance being configured to permit formation of a cavityin said pad of a depth sufficient to at least one of: assist in holdinga patient on a surgical procedure table, and assist in minimizingundesired movement of a body of a patient on a surgical procedure table,during a surgical procedure performed while a patient is in a surgicalposition; said pad being configured to generate a sufficient staticfrictional force on skin of a patient on said pad to stabilize a patienton said pad; said pad being configured to generate a friction orfriction-like force due to formation of a cavity in said pad, and whichforce generated by said coefficient of static friction both togetherbeing sufficient to hold a body of a patient substantially static on asurgical procedure table; wherein a holding quality or ability betweensaid pad and a patient is a combination of the coefficient of frictionbetween a patient and said pad and the holding ability of the impressionmade by a patient in said pad; said holding quality or abilitycomprising an equivalent total frictional characteristic including thefriction due to the coefficient of friction and the friction orfriction-like force due to the pad deformation; said pad furthercomprising a viscoelastic foam in which an impression is formed and heldin the foam at least for a time after a patient is moved from oneposition to another or from an operating table; and said viscoelasticfoam also provides an air flow sufficient to provide substantial airflow at the skin of a patient in contact with said viscoelastic foam;and wherein said air flow of said open cell foam is in the range of oneof i) and ii), wherein i) and ii) are: i) 0.1 to 3.0 cubic foot perminute; and ii) 0.3 to 1.0 cubic foot per minute.
 3. The single use padpatient support system according to claim 2, wherein said single use padpatient support system comprises a single layer of viscoelastic foamconfigured to make direct contact with a surgical procedure table anddirect contact with at least a portion of a patient's skin.
 4. Thesingle use pad patient support system according to claim 3, wherein saidequivalent total frictional characteristic is sufficient to hold apatient on a surgical procedure table at an inclination of at leastabout 25 degrees.
 5. The single use pad patient support system accordingto claim 2, wherein said equivalent total frictional characteristic issufficient to hold a patient on a surgical procedure table at aninclination of at least about 15 degrees.
 6. The single use pad patientsupport system according to claim 5, wherein said pad comprises atensile strength sufficient to minimize tearing of said pad.
 7. Thesingle use pad patient support system according to claim 6, wherein saidviscoelastic foam comprises: a rebound, such as ball rebound, beingsufficiently small to minimize undesirable movement of a patient duringa medical procedure; an indentation force deflection sufficient topermit formation of a depression having a depth sufficient to at leastassist in holding a patient on a medical procedure table; and a tensilestrength sufficient to minimize tearing of said deformable material. 8.The single use pad patient support system according to claim 7, wherein:said ball rebound is in the range of approximately 0.1 percent toapproximately 5 percent; said indentation force deflection is in therange of approximately 7 to approximately 18 pounds; said tensilestrength is in the range of approximately 5 pounds per square inch toapproximately 15 pounds per square inch; and said viscoelastic foamfurther comprises: a compression set, for a 25 percent compression, ofless than approximately one percent; and a density in the range ofapproximately 75 kilograms per cubic meter to approximately 110kilograms per cubic meter.
 9. The single use pad patient support systemaccording to claim 8, wherein: said ball rebound is in the range ofapproximately 0.1 percent to approximately 1.9 percent; said indentationforce deflection is in the range of approximately 10 to approximately 15pounds; said tensile strength is in the range of approximately 8 poundsper square inch to approximately 12 pounds per square inch; and saidviscoelastic foam further comprises: a compression set, for a 25 percentcompression, which is less than approximately 0.3 percent; and a densityin the range of approximately 83 kilograms per cubic meter toapproximately 103 kilograms per cubic meter; said pad is sufficientlythick to permit formation of a depression having portions of differentdepths, such that the depths of the portions of the depression formed bya buttocks and scapular region of a torso of a patient are greater thanthe depths of other portions of the depression, and such that the deeperportions of the depression provide a greater portion of the holdingforces than shallower portions of the depression; said single use padpatient support system comprises a retaining arrangement configured toat least assist in the retention of said single use pad patient supportsystem on a surgical procedure table; and said pad has a thickness inthe range of from approximately three-fourths of an inch to three inchesor greater.
 10. The single use pad patient support system according toclaim 2, wherein said equivalent total frictional characteristic issufficient to hold a patient on a surgical procedure table at aninclination of at least about 20 degrees.
 11. The single use pad patientsupport system according to claim 2, wherein said equivalent totalfrictional characteristic is sufficient to hold a patient on a surgicalprocedure table at an inclination of at least about 30 degrees.
 12. Thesingle use pad patient support system according to claim 2, wherein saidequivalent total frictional characteristic is sufficient to hold apatient on a surgical procedure table at an inclination of at leastabout 35 degrees.
 13. The single use pad patient support systemaccording to claim 2, wherein said equivalent total frictionalcharacteristic is sufficient to hold a patient on a surgical proceduretable at an inclination of at least about 40 degrees.
 14. The single usepad patient support system according to claim 2, wherein said equivalenttotal frictional characteristic is sufficient to hold a patient on asurgical procedure table at an inclination of at least about 45 degrees.15. A patient support system configured to minimize injuries caused bypressure on portions of a body of a patient and minimize unwantedmovement of a patient upon a patient being in surgical position on asurgical procedure table, such as a surgical operating table or apatient examination table, said patient support system comprising a pad;said pad comprising: a viscoelastic, polyurethane open cell foamcomprising a coefficient of static friction in the range of 0.2 to 1.0and said coefficient of static friction bring sufficient to assist inminimizing movement of said pad on a surgical procedure table upon apatient being on a surgical procedure table; sufficient thickness tosufficiently cushion a body of a patient to: minimize bottoming out orprevent bottoming out, on a surgical procedure table, of one or more ofportions of a body of a patient during positioning of a patient andduring a surgical procedure, and to minimize injuries from pressure on apatient during a surgical procedure; and sufficient compliance toconform to a substantial portion of a body of a patient; sufficientthinness to stabilize a patient on a surgical procedure table; and saidsufficient thickness and said sufficient compliance being configured topermit formation of a cavity in said pad of a depth sufficient to atleast one of: assist in holding a patient on a surgical procedure table,and assist in minimizing undesired movement of a body of a patient on asurgical procure table, during a surgical procedure performed while apatient is in a surgical position; wherein said pad is configured togenerate a sufficient static frictional force on skin of a patient on asurgical procedure table pad to stabilize a patient on a surgicalprocedure table pad; said pad is configured to generate a friction orfriction-like force due to the formation of a cavity in saidviscoelastic foam pad, and which force generated by said coefficient ofstatic friction both together being sufficient to hold a body of apatient substantially static on a surgical procedure table; wherein aholding quality or ability between said pad and a patient is acombination of the coefficient of friction between a patient and saidpad and the holding ability of the impression made by a patient in saidpad; said holding quality or ability comprising an equivalent totalfrictional characteristic including the friction due to the coefficientof friction and the friction or friction-like force due to the paddeformation; and said viscoelastic foam pad comprises a viscoelasticfoam in which an impression is formed and held in the foam at least fora time after a patient is moved from one position to another or from asurgical table; in which said viscoelastic, polyurethane open cell foamalso provides an air flow sufficient to provide substantial air flow atat least a portion of a contact area of a patient; and wherein said airflow of said viscoelastic foam is in the range of one of i) and ii),wherein i) and ii) are: i) 0.1 to 3.0 cubic foot per minute; and ii) 0.3to 1.0 cubic foot per minute.
 16. The patient support system accordingto claim 15, wherein said viscoelastic foam comprises: a rebound, suchas ball rebound, being sufficiently small to minimize undesirablemovement of a patient during a medical procedure; an indentation forcedeflection sufficient to permit formation of a depression having a depthsufficient to at least assist in holding a patient on a medicalprocedure table; and a tensile strength sufficient to minimize tearingof said deformable material.
 17. The patient support system according toclaim 16, wherein: said ball rebound is in the range of approximately0.1 percent to approximately 5 percent; said indentation forcedeflection is in the range of approximately 7 to approximately 18pounds; said tensile strength is in the range of approximately 5 poundsper square inch to approximately 15 pounds per square inch; and saidviscoelastic foam further comprises: a compression set, for a 25 percentcompression, of less than approximately one percent; and a density inthe range of approximately 75 kilograms per cubic meter to approximately110 kilograms per cubic meter.
 18. The patient support system accordingto claim 17, wherein: said ball rebound is in the range of approximately0.1 percent to approximately 1.9 percent; said indentation forcedeflection is in the range of approximately 10 to approximately 15pounds; said tensile strength is in the range of approximately 8 poundsper square inch to approximately 12 pounds per square inch; and saidviscoelastic foam further comprises: a compression set, for a 25 percentcompression, which is less than approximately 0.3 percent; and a densityin the range of approximately 83 kilograms per cubic meter toapproximately 103 kilograms per cubic meter; said pad is sufficientlythick to permit formation of a depression having portions of differentdepths, such that the depths of the portions of the depression formed bya buttocks and scapular region of a torso of a patient are greater thanthe depths of other portions of the depression, and such that the deeperportions of the depression provide a greater portion of the holdingforces than shallower portions of the depression; said patient supportsystem comprises a retaining arrangement configured to at least assistin the retention of said patient support system on a surgical proceduretable; and said pad has a thickness in the range of from approximatelythree-fourths of an inch to three inches or greater.